EMBO Molecular Medicine (Dec 2022)

Sex differences and risk factors for bleeding in Alagille syndrome

  • Simona Hankeova,
  • Noemi Van Hul,
  • Jakub Laznovsky,
  • Elisabeth Verboven,
  • Katrin Mangold,
  • Naomi Hensens,
  • Csaba Adori,
  • Elvira Verhoef,
  • Tomas Zikmund,
  • Feven Dawit,
  • Michaela Kavkova,
  • Jakub Salplachta,
  • Marika Sjöqvist,
  • Bengt R Johansson,
  • Mohamed G Hassan,
  • Linda Fredriksson,
  • Karsten Baumgärtel,
  • Vitezslav Bryja,
  • Urban Lendahl,
  • Andrew Jheon,
  • Florian Alten,
  • Kristina Teär Fahnehjelm,
  • Björn Fischler,
  • Jozef Kaiser,
  • Emma R Andersson

DOI
https://doi.org/10.15252/emmm.202215809
Journal volume & issue
Vol. 14, no. 12
pp. n/a – n/a

Abstract

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Abstract Spontaneous bleeds are a leading cause of death in the pediatric JAG1‐related liver disease Alagille syndrome (ALGS). We asked whether there are sex differences in bleeding events in patients, whether Jag1Ndr/Ndr mice display bleeds or vascular defects, and whether discovered vascular pathology can be confirmed in patients non‐invasively. We performed a systematic review of patients with ALGS and vascular events following PRISMA guidelines, in the context of patient sex, and found significantly more girls than boys reported with spontaneous intracranial hemorrhage. We investigated vascular development, homeostasis, and bleeding in Jag1Ndr/Ndr mice, using retina as a model. Jag1Ndr/Ndr mice displayed sporadic brain bleeds, a thin skull, tortuous blood vessels, sparse arterial smooth muscle cell coverage in multiple organs, which could be aggravated by hypertension, and sex‐specific venous defects. Importantly, we demonstrated that retinographs from patients display similar characteristics with significantly increased vascular tortuosity. In conclusion, there are clinically important sex differences in vascular disease in ALGS, and retinography allows non‐invasive vascular analysis in patients. Finally, Jag1Ndr/Ndr mice represent a new model for vascular compromise in ALGS.

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